Surgical staple cartridge with varying staple crown width along a curve

ABSTRACT

A surgical instrument includes an end effector with a staple cartridge. The end effector and staple cartridge extend along a centerline and have an arcuate portion. The staple cartridge includes a deck and a plurality of staples. The plurality of staples include an outer set of staples and an inner set of staples for respective receipt within outer and inner rows of staple openings formed through the deck. At least one staple of the outer set of staples has an elongated crown relative to the inner set of staples such that the outer set of staples are configured to overlap with the inner set of staples in a direction transverse to the centerline.

BACKGROUND

In some settings, endoscopic surgical instruments may be preferred overtraditional open surgical devices since a smaller incision may reducethe post-operative recovery time and complications. Consequently, someendoscopic surgical instruments may be suitable for placement of adistal end effector at a desired surgical site through the cannula of atrocar. These distal end effectors may engage tissue in a number of waysto achieve a diagnostic or therapeutic effect (e.g., endocutter,grasper, cutter, stapler, clip applier, access device, drug/gene therapydelivery device, and energy delivery device using ultrasonic vibration,RF, laser, etc.). Endoscopic surgical instruments may include a shaftbetween the end effector and a handle portion, which is manipulated bythe clinician. Such a shaft may enable insertion to a desired depth androtation about the longitudinal axis of the shaft, thereby facilitatingpositioning of the end effector within the patient. Positioning of anend effector may be further facilitated through inclusion of one or morearticulation joints or features, enabling the end effector to beselectively articulated or otherwise deflected relative to thelongitudinal axis of the shaft.

Examples of endoscopic surgical instruments include surgical staplers.Some such staplers are operable to clamp down on layers of tissue, cutthrough the clamped layers of tissue, and drive staples through thelayers of tissue to substantially seal the severed layers of tissuetogether near the severed ends of the tissue layers. Merely exemplarysurgical staplers are disclosed in U.S. Pat. No. 4,805,823, entitled“Pocket Configuration for Internal Organ Staplers,” issued Feb. 21,1989; U.S. Pat. No. 5,415,334, entitled “Surgical Stapler and StapleCartridge,” issued May 16, 1995; U.S. Pat. No. 5,465,895, entitled“Surgical Stapler Instrument,” issued Nov. 14, 1995; U.S. Pat. No.5,597,107, entitled “Surgical Stapler Instrument,” issued Jan. 28, 1997;U.S. Pat. No. 5,632,432, entitled “Surgical Instrument,” issued May 27,1997; U.S. Pat. No. 5,673,840, entitled “Surgical Instrument,” issuedOct. 7, 1997; U.S. Pat. No. 5,704,534, entitled “Articulation Assemblyfor Surgical Instruments,” issued Jan. 6, 1998; U.S. Pat. No. 5,814,055,entitled “Surgical Clamping Mechanism,” issued Sep. 29, 1998; U.S. Pat.No. 6,978,921, entitled “Surgical Stapling Instrument Incorporating anE-Beam Firing Mechanism,” issued Dec. 27, 2005; U.S. Pat. No. 7,000,818,entitled “Surgical Stapling Instrument Having Separate Distinct Closingand Firing Systems,” issued Feb. 21, 2006; U.S. Pat. No. 7,143,923,entitled “Surgical Stapling Instrument Having a Firing Lockout for anUnclosed Anvil,” issued Dec. 5, 2006; U.S. Pat. No. 7,303,108, entitled“Surgical Stapling Instrument Incorporating a Multi-Stroke FiringMechanism with a Flexible Rack,” issued Dec. 4, 2007; U.S. Pat. No.7,367,485, entitled “Surgical Stapling Instrument Incorporating aMultistroke Firing Mechanism Having a Rotary Transmission,” issued May6, 2008; U.S. Pat. No. 7,380,695, entitled “Surgical Stapling InstrumentHaving a Single Lockout Mechanism for Prevention of Firing,” issued Jun.3, 2008; U.S. Pat. No. 7,380,696, entitled “Articulating SurgicalStapling Instrument Incorporating a Two-Piece E-Beam Firing Mechanism,”issued Jun. 3, 2008; U.S. Pat. No. 7,404,508, entitled “SurgicalStapling and Cutting Device,” issued Jul. 29, 2008; U.S. Pat. No.7,434,715, entitled “Surgical Stapling Instrument Having MultistrokeFiring with Opening Lockout,” issued Oct. 14, 2008; U.S. Pat. No.7,721,930, entitled “Disposable Cartridge with Adhesive for Use with aStapling Device,” issued May 25, 2010; U.S. Pat. No. 8,408,439, entitled“Surgical Stapling Instrument with An Articulatable End Effector,”issued Apr. 2, 2013; and U.S. Pat. No. 8,453,914, entitled “Motor-DrivenSurgical Cutting Instrument with Electric Actuator Directional ControlAssembly,” issued Jun. 4, 2013. The disclosure of each of theabove-cited U.S. patents is incorporated by reference herein.

While the surgical staplers referred to above are described as beingused in endoscopic procedures, it should be understood that suchsurgical staplers may also be used in open procedures and/or othernon-endoscopic procedures. By way of example only, a surgical staplermay be inserted through a thoracotomy, and thereby between a patient'sribs, to reach one or more organs in a thoracic surgical procedure thatdoes not use a trocar as a conduit for the stapler. Such procedures mayinclude the use of the stapler to sever and close a vessel leading to alung. For instance, the vessels leading to an organ may be severed andclosed by a stapler before removal of the organ from the thoraciccavity. Of course, surgical staplers may be used in various othersettings and procedures.

Examples of surgical staplers that may be particularly suited or usethrough a thoracotomy are disclosed in U.S. patent application Ser. No.14/810,786, entitled “Surgical Staple Cartridge with Compression Featureat Knife Slot,” filed Jul. 29, 2015; U.S. Patent Pub. No. 2014/0243801,entitled “Surgical Instrument End Effector Articulation Drive withPinion and Opposing Racks,” published Aug. 28, 2014; U.S. Patent Pub.No. 2014/0239041, entitled “Lockout Feature for Movable Cutting Memberof Surgical Instrument,” published Aug. 28, 2014; U.S. Patent Pub. No.2014/0239042, entitled “Integrated Tissue Positioning and Jaw AlignmentFeatures for Surgical Stapler,” published Aug. 28, 2014; U.S. PatentPub. No. 2014/0239036, entitled “Jaw Closure Feature for End Effector ofSurgical Instrument,” published Aug. 28, 2014; U.S. Patent Pub. No.2014/0239040, entitled “Surgical Instrument with Articulation Lockhaving a Detenting Binary Spring,” published Aug. 28, 2014; U.S. PatentPub. No. 2014/0239043, entitled “Distal Tip Features for End Effector ofSurgical Instrument,” published Aug. 28, 2014; U.S. Patent Pub. No.2014/0239037, entitled “Staple Forming Features for Surgical StaplingInstrument,” published Aug. 28, 2014; U.S. Patent Pub. No. 2014/0239038,entitled “Surgical Instrument with Multi-Diameter Shaft,” published Aug.28, 2014; and U.S. Patent Pub. No. 2014/0239044, entitled “InstallationFeatures for Surgical Instrument End Effector Cartridge,” published Aug.28, 2014. The disclosure of each of the above-cited U.S. patentapplications is incorporated by reference herein.

While various kinds of surgical stapling instruments and associatedcomponents have been made and used, it is believed that no one prior tothe inventor(s) has made or used the invention described in the appendedclaims.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute apart of this specification, illustrate embodiments of the invention,and, together with the general description of the invention given above,and the detailed description of the embodiments given below, serve toexplain the principles of the present invention.

FIG. 1 depicts a perspective view of an exemplary articulating surgicalstapling instrument;

FIG. 2 depicts a side elevational view of the instrument of FIG. 1;

FIG. 3 depicts a perspective view of an end effector of the instrumentof FIG. 1, with the end effector in a closed configuration;

FIG. 4 depicts a perspective view of the end effector of FIG. 3, withthe end effector in an open configuration;

FIG. 5 depicts an exploded perspective view of the end effector of FIG.3;

FIG. 6 depicts a cross-sectional end view of the end effector of FIG. 3,taken along line 6-6 of FIG. 4;

FIG. 7A depicts a cross-sectional side view of the end effector of FIG.3, taken along line 7-7 of FIG. 4, with a firing beam in a proximalposition;

FIG. 7B depicts a cross-sectional side view of the end effector of FIG.3, taken along line 7-7 of FIG. 4, with the firing beam in a distalposition;

FIG. 8 depicts a perspective view of the end effector of FIG. 3,positioned at tissue and having been actuated once in the tissue;

FIG. 9 depicts a side elevational view of another exemplary articulatingsurgical stapling instrument;

FIG. 10 depicts a perspective view of an end effector of the instrumentof FIG. 9, with the end effector in an open configuration;

FIG. 11 depicts a top view of a lower jaw of the end effector of FIG.10;

FIG. 12 depicts a bottom view of an upper jaw of the end effector ofFIG. 10;

FIG. 13 depicts an exploded perspective view of the lower jaw of FIG.11;

FIG. 14 depicts a top view of the lower jaw of FIG. 11;

FIG. 15A depicts a schematic representation of a liver having a vesselextending through the liver tissue;

FIG. 15B depicts the schematic representation of the end effector ofFIG. 10 severing the liver tissue of FIG. 15A;

FIG. 15C depicts the schematic representation of the vessel of FIG. 15Bexposed from the severed liver tissue of FIG. 15A;

FIG. 15D depicts the schematic representation of the end effector ofFIG. 10 stapling the exposed vessel of FIG. 15C;

FIG. 15E depicts the schematic representation of the vessel of FIG. 15Dexposed and stapled; and

FIG. 15F depicts the schematic representation of the liver of FIG. 15Ahaving a portion of the liver tissue and the vessel resected therefrom.

The drawings are not intended to be limiting in any way, and it iscontemplated that various embodiments of the invention may be carriedout in a variety of other ways, including those not necessarily depictedin the drawings. The accompanying drawings incorporated in and forming apart of the specification illustrate several aspects of the presentinvention, and together with the description serve to explain theprinciples of the invention; it being understood, however, that thisinvention is not limited to the precise arrangements shown.

DETAILED DESCRIPTION

The following description of certain examples of the invention shouldnot be used to limit the scope of the present invention. Other examples,features, aspects, embodiments, and advantages of the invention willbecome apparent to those skilled in the art from the followingdescription, which is by way of illustration, one of the best modescontemplated for carrying out the invention. As will be realized, theinvention is capable of other different and obvious aspects, all withoutdeparting from the invention. Accordingly, the drawings and descriptionsshould be regarded as illustrative in nature and not restrictive.

I. Exemplary Surgical Stapler

FIG. 1 depicts an exemplary surgical stapling and severing instrument(10) that includes a handle assembly (20), a shaft assembly (30), and anend effector (40). End effector (40) and the distal portion of shaftassembly (30) are sized for insertion, in a nonarticulated state asdepicted in FIG. 1, through a trocar cannula to a surgical site in apatient for performing a surgical procedure. By way of example only,such a trocar may be inserted in a patient's abdomen, between two of thepatient's ribs, or elsewhere. In some settings, instrument (10) is usedwithout a trocar. For instance, end effector (40) and the distal portionof shaft assembly (30) may be inserted directly through a thoracotomy orother type of incision. It should be understood that terms such as“proximal” and “distal” are used herein with reference to a cliniciangripping handle assembly (20) of instrument (10). Thus, end effector(40) is distal with respect to the more proximal handle assembly (20).It will be further appreciated that for convenience and clarity, spatialterms such as “vertical” and “horizontal” are used herein with respectto the drawings. However, surgical instruments are used in manyorientations and positions, and these terms are not intended to belimiting and absolute.

A. Exemplary Handle Assembly and Shaft Assembly

As shown in FIGS. 1-2, handle assembly (20) of the present examplecomprises pistol grip (22), a closure trigger (24), and a firing trigger(26). Each trigger (24, 26) is selectively pivotable toward and awayfrom pistol grip (22) as will be described in greater detail below.Handle assembly (20) further includes an anvil release button (25), afiring beam reverse switch (27), and a removable battery pack (28).These components will also be described in greater detail below. Ofcourse, handle assembly (20) may have a variety of other components,features, and operabilities, in addition to or in lieu of any of thosenoted above. Other suitable configurations for handle assembly (20) willbe apparent to those of ordinary skill in the art in view of theteachings herein.

As shown in FIGS. 1-3, shaft assembly (30) of the present examplecomprises an outer closure tube (32), an articulation section (34), anda closure ring (36), which is further coupled with end effector (40).Closure tube (32) extends along the length of shaft assembly (30).Closure ring (36) is positioned distal to articulation section (34).Closure tube (32) and closure ring (36) are configured to translatelongitudinally relative to handle assembly (20). Longitudinaltranslation of closure tube (32) is communicated to closure ring (36)via articulation section (34). Exemplary features that may be used toprovide longitudinal translation of closure tube (32) and closure ring(36) will be described in greater detail below.

Articulation section (34) is operable to laterally deflect closure ring(36) and end effector (40) laterally away from the longitudinal axis(LA) of shaft assembly (30) at a desired angle (a). End effector (40)may thereby reach behind an organ or approach tissue from a desiredangle or for other reasons. In some versions, articulation section (34)enables deflection of end effector (40) along a single plane. In someother versions, articulation section (34) enables deflection of endeffector along more than one plane. In the present example, articulationis controlled through an articulation control knob (35) which is locatedat the proximal end of shaft assembly (30). Knob (35) is rotatable aboutan axis that is perpendicular to the longitudinal axis (LA) of shaftassembly (30). Closure ring (36) and end effector (40) pivot about anaxis that is perpendicular to the longitudinal axis (LA) of shaftassembly (30) in response to rotation of knob (35). By way of exampleonly, rotation of knob (35) clockwise may cause corresponding clockwisepivoting of closure ring (36) and end effector (40) at articulationsection (34). Articulation section (34) is configured to communicatelongitudinal translation of closure tube (32) to closure ring (36),regardless of whether articulation section (34) is in a straightconfiguration or an articulated configuration.

In some versions, articulation section (34) and/or articulation controlknob (35) are/is constructed and operable in accordance with at leastsome of the teachings of U.S. Pub. No. 2014/0243801, entitled “SurgicalInstrument End Effector Articulation Drive with Pinion and OpposingRacks,” published Aug. 28, 2014, the disclosure of which is incorporatedby reference herein. Articulation section (34) may also be constructedand operable in accordance with at least some of the teachings of U.S.patent application Ser. No. 14/314,125, entitled “Articulation DriveFeatures for Surgical Stapler,” filed Jun. 25, 2014, the disclosure ofwhich is incorporated by reference herein; and/or in accordance with thevarious teachings below. Other suitable forms that articulation section(34) and articulation knob (35) may take will be apparent to those ofordinary skill in the art in view of the teachings herein.

As shown in FIGS. 1-2, shaft assembly (30) of the present examplefurther includes a rotation knob (31). Rotation knob (31) is operable torotate the entire shaft assembly (30) and end effector (40) relative tohandle assembly (20) about the longitudinal axis (LA) of shaft assembly(30). In some versions, rotation knob (31) is operable to selectivelylock the angular position of shaft assembly (30) and end effector (40)relative to handle assembly (20) about the longitudinal axis (LA) ofshaft assembly (30). For instance, rotation knob (31) may betranslatable between a first longitudinal position, in which shaftassembly (30) and end effector (40) are rotatable relative to handleassembly (20) about the longitudinal axis (LA) of shaft assembly (30);and a second longitudinal position, in which shaft assembly (30) and endeffector (40) are not rotatable relative to handle assembly (20) aboutthe longitudinal axis (LA) of shaft assembly (30). Of course, shaftassembly (30) may have a variety of other components, features, andoperabilities, in addition to or in lieu of any of those noted above. Byway of example only, at least part of shaft assembly (30) is constructedin accordance with at least some of the teachings of U.S. Pub. No.2014/0239038, entitled “Surgical Instrument with Multi-Diameter Shaft,”published Aug. 28, 2014, the disclosure of which is incorporated byreference herein. Other suitable configurations for shaft assembly (30)will be apparent to those of ordinary skill in the art in view of theteachings herein.

B. Exemplary End Effector

As also shown in FIGS. 3-5, end effector (40) of the present exampleincludes a lower jaw (50) and a pivotable anvil (60). Anvil (60)includes a pair of integral, outwardly extending pins (66) that aredisposed in corresponding curved slots (54) of lower jaw (50). Anvil(60) is pivotable toward and away from lower jaw (50) between an openposition (shown in FIGS. 2 and 4) and a closed position (shown in FIGS.1, 3, and 7A-7B). Use of the term “pivotable” (and similar terms with“pivot” as a base) should not be read as necessarily requiring pivotalmovement about a fixed axis. For instance, in the present example, anvil(60) pivots about an axis that is defined by pins (66), which slidealong curved slots (54) of lower jaw (50) as anvil (60) moves towardlower jaw (50). In such versions, the pivot axis translates along thepath defined by slots (54) while anvil (60) simultaneously pivots aboutthat axis. In addition or in the alternative, the pivot axis may slidealong slots (54) first, with anvil (60) then pivoting about the pivotaxis after the pivot axis has slid a certain distance along the slots(54). It should be understood that such sliding/translating pivotalmovement is encompassed within terms such as “pivot,” “pivots,”“pivotal,” “pivotable,” “pivoting,” and the like. Of course, someversions may provide pivotal movement of anvil (60) about an axis thatremains fixed and does not translate within a slot or channel, etc.

As best seen in FIG. 5, lower jaw (50) of the present example defines achannel (52) that is configured to receive a staple cartridge (70).Staple cartridge (70) may be inserted into channel (52), end effector(40) may be actuated, and then staple cartridge (70) may be removed andreplaced with another staple cartridge (70). Lower jaw (50) thusreleasably retains staple cartridge (70) in alignment with anvil (60)for actuation of end effector (40). In some versions, lower jaw (50) isconstructed in accordance with at least some of the teachings of U.S.Pub. No. 2014/0239044, entitled “Installation Features for SurgicalInstrument End Effector Cartridge,” published Aug. 28, 2014, thedisclosure of which is incorporated by reference herein. Other suitableforms that lower jaw (50) may take will be apparent to those of ordinaryskill in the art in view of the teachings herein.

As best seen in FIGS. 4-6, staple cartridge (70) of the present examplecomprises a cartridge body (71) and a tray (76) secured to the undersideof cartridge body (71). The upper side of cartridge body (71) presents adeck (73), against which tissue may be compressed when anvil (60) is ina closed position. Cartridge body (71) further defines a longitudinallyextending channel (72) and a plurality of staple pockets (74). A staple(77) is positioned in each staple pocket (74). A staple driver (75) isalso positioned in each staple pocket (74), underneath a correspondingstaple (77), and above tray (76). As will be described in greater detailbelow, staple drivers (75) are operable to translate upwardly in staplepockets (74) to thereby drive staples (77) upwardly through staplepockets (74) and into engagement with anvil (60). Staple drivers (75)are driven upwardly by a wedge sled (78), which is captured betweencartridge body (71) and tray (76), and which translates longitudinallythrough cartridge body (71). Wedge sled (78) includes a pair ofobliquely angled cam surfaces (79), which are configured to engagestaple drivers (75) and thereby drive staple drivers (75) upwardly aswedge sled (78) translates longitudinally through cartridge (70). Forinstance, when wedge sled (78) is in a proximal position as shown inFIG. 7A, staple drivers (75) are in downward positions and staples (77)are located in staple pockets (74). As wedge sled (78) is driven to thedistal position shown in FIG. 7B by a translating knife member (80),wedge sled (78) drives staple drivers (75) upwardly, thereby drivingstaples (77) out of staple pockets (74) and into staple forming pockets(64). Thus, staple drivers (75) translate along a vertical dimension aswedge sled (78) translates along a horizontal dimension.

It should be understood that the configuration of staple cartridge (70)may be varied in numerous ways. For instance, staple cartridge (70) ofthe present example includes two longitudinally extending rows of staplepockets (74) on one side of channel (72); and another set of twolongitudinally extending rows of staple pockets (74) on the other sideof channel (72). However, in some other versions, staple cartridge (70)includes three, one, or some other number of staple pockets (74) on eachside of channel (72). In some versions, staple cartridge (70) isconstructed and operable in accordance with at least some of theteachings of U.S. Pub. No. 2014/0239042, entitled “Integrated TissuePositioning and Jaw Alignment Features for Surgical Stapler,” publishedAug. 28, 2014, the disclosure of which is incorporated by referenceherein. In addition or in the alternative, staple cartridge (70) may beconstructed and operable in accordance with at least some of theteachings of U.S. Pub. No. 2014/0239044, entitled “Installation Featuresfor Surgical Instrument End Effector Cartridge,” published Aug. 28,2014, the disclosure of which is incorporated by reference herein. Othersuitable forms that staple cartridge (70) may take will be apparent tothose of ordinary skill in the art in view of the teachings herein.

As best seen in FIG. 4, anvil (60) of the present example comprises alongitudinally extending channel (62) and a plurality of staple formingpockets (64). Channel (62) is configured to align with channel (72) ofstaple cartridge (70) when anvil (60) is in a closed position. Eachstaple forming pocket (64) is positioned to lie over a correspondingstaple pocket (74) of staple cartridge (70) when anvil (60) is in aclosed position. Staple forming pockets (64) are configured to deformthe legs of staples (77) when staples (77) are driven through tissue andinto anvil (60). In particular, staple forming pockets (64) areconfigured to bend the legs of staples (77) to secure the formed staples(77) in the tissue. Anvil (60) may be constructed in accordance with atleast some of the teachings of U.S. Pub. No. 2014/0239042, entitled“Integrated Tissue Positioning and Jaw Alignment Features for SurgicalStapler,” published Aug. 28, 2014; at least some of the teachings ofU.S. Pub. No. 2014/0239036, entitled “Jaw Closure Feature for EndEffector of Surgical Instrument,” published Aug. 28, 2014; and/or atleast some of the teachings of U.S. Pub. No. 2014/0239037, entitled“Staple Forming Features for Surgical Stapling Instrument,” publishedAug. 28, 2014, the disclosure of which is incorporated by referenceherein. Other suitable forms that anvil (60) may take will be apparentto those of ordinary skill in the art in view of the teachings herein.

In the present example, knife member (80) is configured to translatethrough end effector (40). As best seen in FIGS. 5 and 7A-7B, knifemember (80) is secured to the distal end of a firing beam (82), whichextends through a portion of shaft assembly (30). As best seen in FIGS.4 and 6, knife member (80) is positioned in channels (62, 72) of anvil(60) and staple cartridge (70). Knife member (80) includes a distallypresented cutting edge (84) that is configured to sever tissue that iscompressed between anvil (60) and deck (73) of staple cartridge (70) asknife member (80) translates distally through end effector (40). Asnoted above and as shown in FIGS. 7A-7B, knife member (80) also driveswedge sled (78) distally as knife member (80) translates distallythrough end effector (40), thereby driving staples (77) through tissueand against anvil (60) into formation. Various features that may be usedto drive knife member (80) distally through end effector (40) will bedescribed in greater detail below.

In some versions, end effector (40) includes lockout features that areconfigured to prevent knife member (80) from advancing distally throughend effector (40) when a staple cartridge (70) is not inserted in lowerjaw (50). In addition or in the alternative, end effector (40) mayinclude lockout features that are configured to prevent knife member(80) from advancing distally through end effector (40) when a staplecartridge (70) that has already been actuated once (e.g., with allstaples (77) deployed therefrom) is inserted in lower jaw (50). By wayof example only, such lockout features may be configured in accordancewith at least some of the teachings of U.S. Pub. No. 2014/0239041,entitled “Lockout Feature for Movable Cutting Member of SurgicalInstrument,” published Aug. 28, 2014, the disclosure of which isincorporated by reference herein; and/or at least some of the teachingsof U.S. patent application Ser. No. 14/314,108, entitled “Method ofUsing Lockout Features for Surgical Staple cartridge,” filed on Jun. 25,2014, the disclosure of which is incorporated by reference herein. Othersuitable forms that lockout features may take will be apparent to thoseof ordinary skill in the art in view of the teachings herein.Alternatively, end effector (40) may simply omit such lockout features.

C. Exemplary Actuation of Anvil

In the present example, anvil (60) is driven toward lower jaw (50) byadvancing closure ring (36) distally relative to end effector (40).Closure ring (36) cooperates with anvil (60) through a camming action todrive anvil (60) toward lower jaw (50) in response to distal translationof closure ring (36) relative to end effector (40). Similarly, closurering (36) may cooperate with anvil (60) to open anvil (60) away fromlower jaw (50) in response to proximal translation of closure ring (36)relative to end effector (40). By way of example only, closure ring (36)and anvil (60) may interact in accordance with at least some of theteachings of U.S. Pub. No. 2014/0239036, entitled “Jaw Closure Featurefor End Effector of Surgical Instrument,” published Aug. 28, 2014, thedisclosure of which is incorporated by reference herein; and/or inaccordance with at least some of the teachings of U.S. patentapplication Ser. No. 14/314,108, entitled “Jaw Opening Feature forSurgical Stapler,” filed on Jun. 25, 2014, the disclosure of which isincorporated by reference herein. Exemplary features that may be used toprovide longitudinal translation of closure ring (36) relative to endeffector (40) will be described in greater detail below.

As noted above, handle assembly (20) includes pistol grip (22) andclosure trigger (24). As also noted above, anvil (60) is closed towardlower jaw (50) in response to distal advancement of closure ring (36).In the present example, closure trigger (24) is pivotable toward pistolgrip (22) to drive closure tube (32) and closure ring (36) distally.Various suitable components that may be used to convert pivotal movementof closure trigger (24) toward pistol grip (22) into distal translationof closure tube (32) and closure ring (36) relative to handle assembly(20) will be apparent to those of ordinary skill in the art in view ofthe teachings herein. When closure trigger (24) reaches a fully pivotedstate, such that anvil (60) is in a fully closed position relative tolower jaw (50), locking features in handle assembly (20) lock theposition of closure trigger (24) and closure tube (32), thereby lockinganvil (60) in a fully closed position relative to lower jaw (50). Theselocking features are released by actuation of anvil release button (25).Anvil release button (25) is configured and positioned to be actuated bythe thumb of the operator hand that grasps pistol grip (22). In otherwords, the operator may grasp pistol grip (22) with one hand, actuateclosure trigger (24) with one or more fingers of the same hand, and thenactuate anvil release button (25) with the thumb of the same hand,without ever needing to release the grasp of pistol grip (22) with thesame hand. Other suitable features that may be used to actuate anvil(60) will be apparent to those of ordinary skill in the art in view ofthe teachings herein.

D. Exemplary Actuation of Firing Beam

In the present example, instrument (10) provides motorized control offiring beam (82). In particular, instrument (10) includes motorizedcomponents that are configured to drive firing beam (82) distally inresponse to pivoting of firing trigger (26) toward pistol grip (22). Insome versions, a motor (not shown) is contained in pistol grip (22) andreceives power from battery pack (28). This motor is coupled with atransmission assembly (not shown) that converts rotary motion of a driveshaft of the motor into linear translation of firing beam (82). In somesuch versions, firing beam (82) may only be advanced distally when anvil(60) is in a fully closed position relative to lower jaw (50). Afterfiring beam (82) is advanced distally to sever tissue and drive staples(77) as described above with reference to FIGS. 7A-7B, the driveassembly for firing beam (82) may be automatically reversed to drivefiring beam (82) proximally back to the retracted position (e.g., backfrom the position shown in FIG. 7B to the position shown in FIG. 7A).Alternatively, the operator may actuate firing beam reverse switch (27),which may reverse the drive assembly for firing beam (82) in order toretract firing beam (82) to a proximal position. Handle assembly (20) ofthe present example further includes a bailout feature (21), which isoperable to provide a mechanical bailout allowing the operator tomanually retract firing beam (82) proximally (e.g., in the event ofpower loss while firing beam (82) is in a distal position, etc.).

By way of example only, the features that are operable to providemotorized actuation of firing beam (82) may be configured and operablein accordance with at least some of the teachings of U.S. Pat. No.8,210,411, entitled “Motor-Driven Surgical Instrument,” issued Jul. 3,2012, the disclosure of which is incorporated by reference herein. Asanother merely illustrative example, the features that are operable toprovide motorized actuation of firing beam (82) may be configured andoperable in accordance with at least some of the teachings of U.S. Pat.No. 8,453,914, entitled “Motor-Driven Surgical Cutting Instrument withElectric Actuator Directional Control Assembly,” issued Jun. 4, 2013,the disclosure of which is incorporated by reference herein. As yetanother merely illustrative example, the features that are operable toprovide motorized actuation of firing beam (82) may be configured andoperable in accordance with at least some of the teachings of U.S.patent application Ser. No. 14/226,142, entitled “Surgical InstrumentComprising a Sensor System,” filed Mar. 26, 2014, the disclosure ofwhich is incorporated by reference herein.

Other suitable components, features, and configurations that may be usedto provide motorization of firing beam (82) will be apparent to those ofordinary skill in the art in view of the teachings herein. It shouldalso be understood that some other versions may provide manual drivingof firing beam (82), such that a motor may be omitted. By way of exampleonly, firing beam (82) may be manually actuated in accordance with atleast some of the teachings of any other reference cited herein.

FIG. 8 shows end effector (40) having been actuated through a singlestroke through tissue (90). As shown, cutting edge (84) (obscured inFIG. 8) has cut through tissue (90), while staple drivers (75) havedriven two alternating rows of staples (77) through the tissue (90) oneach side of the cut line produced by cutting edge (84). Staples (77)are all oriented substantially parallel to the cut line in this example,though it should be understood that staples (77) may be positioned atany suitable orientations. In the present example, end effector (40) iswithdrawn from the trocar after the first stroke is complete, the spentstaple cartridge (70) is replaced with a new staple cartridge (70), andend effector (40) is then again inserted through the trocar to reach thestapling site for further cutting and stapling. This process may berepeated until the desired amount of cuts and staples (77) have beenprovided. Anvil (60) may need to be closed to facilitate insertion andwithdrawal through the trocar; and anvil (60) may need to be opened tofacilitate replacement of staple cartridge (70).

It should be understood that cutting edge (84) may cut tissuesubstantially contemporaneously with staples (77) being driven throughtissue during each actuation stroke. In the present example, cuttingedge (84) just slightly lags behind driving of staples (77), such thatstaple (77) is driven through the tissue just before cutting edge (84)passes through the same region of tissue, though it should be understoodthat this order may be reversed or that cutting edge (84) may bedirectly synchronized with adjacent staples. While FIG. 8 shows endeffector (40) being actuated in two layers (92, 94) of tissue (90), itshould be understood that end effector (40) may be actuated through asingle layer of tissue (90) or more than two layers (92, 94) of tissue.It should also be understood that the formation and positioning ofstaples (77) adjacent to the cut line produced by cutting edge (84) maysubstantially seal the tissue at the cut line, thereby reducing orpreventing bleeding and/or leaking of other bodily fluids at the cutline. Furthermore, while FIG. 8 shows end effector (40) being actuatedin two substantially flat, apposed planar layers (92, 94) of tissue, itshould be understood that end effector (40) may also be actuated acrossa tubular structure such as a blood vessel, a section of thegastrointestinal tract, etc. FIG. 8 should therefore not be viewed asdemonstrating any limitation on the contemplated uses for end effector(40). Various suitable settings and procedures in which instrument (10)may be used will be apparent to those of ordinary skill in the art inview of the teachings herein.

It should also be understood that any other components or features ofinstrument (10) may be configured and operable in accordance with any ofthe various references cited herein. Additional exemplary modificationsthat may be provided for instrument (10) will be described in greaterdetail below. Various suitable ways in which the below teachings may beincorporated into instrument (10) will be apparent to those of ordinaryskill in the art. Similarly, various suitable ways in which the belowteachings may be combined with various teachings of the references citedherein will be apparent to those of ordinary skill in the art. It shouldalso be understood that the below teachings are not limited toinstrument (10) or devices taught in the references cited herein. Thebelow teachings may be readily applied to various other kinds ofinstruments, including instruments that would not be classified assurgical staplers. Various other suitable devices and settings in whichthe below teachings may be applied will be apparent to those of ordinaryskill in the art in view of the teachings herein.

II. Exemplary Alternative Stapling End Effector

While the above surgical instrument (10) provides one example of an endeffector (40) that may be used to staple and sever tissue within apatient, it will be appreciated that the human body is comprised a widevariety of tissues located in distinct, sometimes difficult to accessregions throughout the patient. For example, a liver includes tissueincluding vessels or ducts passing throughout. In settings where theliver includes a tumor, it may be desirable to resect the portion of theliver containing the tumor. The resection may be anatomic (e.g.,resection of the right or left side of the liver, inclusive of the lobeson that side) or non-anatomic (e.g., resection of just a single lobe orwedge of liver tissue). This resection process may entail at least threekinds of steps—a first step to dissect the tissue (e.g., liverparenchyma) around the vessels or ducts, to thereby isolate or revealthe vessels or ducts; a second step to ligate those vessels or ducts;and a third step to sever the ligated vessels or ducts.

One such method of liver resection includes the well known Kelly clampmethod, where a Kelly style clamp is used to compress the liver tissueand thereby dissect the tissue through a crushing action. However,treatments may require many instruments to accommodate such a widevariety of tissues and vessels or ducts within the human body, therebyadding to the time and complexity associated with assessing the state ofthe tissue, selecting and/or changing instruments, and performing theresection. It may therefore be desirable to provide a surgicalinstrument (210) with an end effector (212) having a pair of crushsurfaces (214, 216) that are configured to sever tissue by crushing thetissue; while also providing an adjacent staple cartridge (218) toselectively ligate one or more vessels or ducts passing through thetissue. Thereby, a single surgical instrument (210) will allow theoperator to more quickly assess the tissue and proceed with furthertissue dissection and/or ligation of vessels and ducts.

Surgical instruments (210) are described below in the context ofdissecting liver tissue (e.g., liver parenchyma) with crush surfaces(214, 216) and using staples to ligate associated vessels or ducts(e.g., portal vein, hepatic vein branches, hepatic artery branches,extrahepatic vessels, etc.). In some instances (e.g., in the case ofhepatic vein branches and hepatic artery branches, etc.), the vessel orduct that is sealed by the staples is exposed when the operator crushesthe liver tissue with surfaces (214, 216). In some other instances(e.g., in the case of the portal vein and extrahepatic vessels, etc.),the vessel or duct that is sealed by the staples is separate from theliver tissue that the operator has crushed with surfaces (214, 216).While the following description of surgical instruments (210) and methodof treatment is provided in the context of liver resection, it will beappreciated that surgical instruments (210) may be alternativelyconfigured to treat any tissue in the human body with similar features.It should also be understood that that the features discussed below maybe readily incorporated into surgical instrument (10) discussed above.To this end, like numbers indicate like features described above ingreater detail.

In the following examples, end effectors (212) apply at least twolaterally spaced apart rows of staples where the staples in one row havethe same height as the staples in another row. In some variations, endeffectors (212) are modified to apply at least two laterally spacedapart rows of staples where the staples in one row have a height that isdifferent from the height of the staples in another row.

A. Exemplary Stapling Instrument with Curved End Effector

FIGS. 9-12 show surgical instrument (210) with end effector (212) havingupper crush surface (214), lower crush surface (216) and staplecartridge (218). Surgical instrument (210) also includes handle assembly(20) and shaft assembly (30) discussed above in greater detail. Exceptas otherwise described below, end effector (212), in conjunction withhandle assembly (20) and shaft assembly (30), is configured and operablesimilar to end effector (40) (see FIG. 1).

End effector (212) of the present example further includes a lower jaw(220) and an upper jaw (222). Upper jaw (222) forms an anvil (224) andis pivotally mounted relative to lower jaw (220) for receiving thetissue therebetween. More particularly, anvil (224) is pivotable towardand away from lower jaw (220) between an open position and a closedposition (e.g., in response to pivotal movement of trigger (24) towardand away from pistol grip (22)). For instance, in the present example,anvil (224) pivots about an axis that is defined by pins (not shown),which slide along curved slots (not shown) of lower jaw (220) as anvil(224) moves toward lower jaw (220). In such versions, the pivot axistranslates along the path defined by slots (not shown) while anvil (224)simultaneously pivots about that axis. In addition or in thealternative, the pivot axis may slide along slots (not shown) first,with anvil (224) then pivoting about the pivot axis after the pivot axisslides a certain distance along the slots (not shown). Alternatively,some versions may provide pivotal movement of anvil (224) about an axisthat remains fixed and does not translate within a slot or channel, etc.

As best seen in FIG. 10 and FIG. 11, lower jaw (220) of the presentexample defines a channel (226) that is configured to receive staplecartridge (218). Staple cartridge (218) may be inserted into channel(226), end effector (212) may be actuated, and then staple cartridge(218) may be removed and replaced with another staple cartridge (218).Lower jaw (220) thus releasably retains staple cartridge (218) inalignment with anvil (224) for actuation of end effector (212). In somealternative versions, the components of staple cartridge (218) are fullyintegrated into lower jaw (220) such that end effector (212) may only beused once. Other suitable forms that lower jaw (220) may take will beapparent to those of ordinary skill in the art in view of the teachingsherein.

End effector (212) is generally shaped for improved access to the tissueduring the surgical procedure. More particularly, end effector (212) hasa linear portion (228) that projects from closure ring (36) and extendsto an arcuate portion (230). Arcuate portion (230) in one example curvestransversely to the right (when viewed from above) relative to thelinear portion (228). However, it will be appreciated that the arcuateportion (230) may alternatively curve transversely to the left (whenviewed from above) relative to the linear portion (228). In any case,lower and upper jaws (220, 222) define the linear and arcuate portions(228, 230) as shown in FIGS. 11-13. In addition, lower and upper jaws(220, 222) are tapered such that the end effector narrows in thetransverse dimension toward a distal tip (232) of the end effector (212)for further access within the tissue. As such, a centerline (233) alonga transverse width of end effector (212) extends longitudinally alongend effector (212) following linear and arcuate portions (228, 230)thereof.

Staple cartridge (218) accommodates the shape of lower and upper jaws(220, 222) by further defining the linear and arcuate portions (228,230) and tapering of end effector (212). To this end, staple cartridge(218) of the present example comprises a cartridge body (234) and a tray(not shown) secured to an underside of cartridge body (234). An upperside of cartridge body (234) presents a deck (238), against which tissuemay be compressed when anvil (224) is in a closed position. In someversions, lower crush surface (216) is positioned along staple cartridge(218). However, it will be appreciated that lower crush surface (216),as well as cooperating upper crush surface (214), may be alternativelypositioned along end effector (212) for severing tissue via compression.

Cartridge body (234) further defines a plurality of staple pockets (242a, 242 b, 242 c) following a predetermined pattern along the centerline(233) of deck (238). More particularly, staple cartridge (218) includestwo longitudinally extending rows of staple pockets (242 a, 242 b, 242c), with a left row on a left side of the centerline (233) and a rightrow and a right side of the centerline (233).

One of a plurality of staples (244 a, 244 b, 244 c) is positioned inrespective staple pockets (242 a, 242 b, 242 c). The left and right rowsof staple pockets (242 a, 242 b, 242 c) are configured to overlap in adirection transverse to the centerline (233) in order to install theplurality of staples (244 a, 244 b, 244 c) within the tissue and inhibitopenings therebetween, for improved ligation. In other words, aconsistent gap (G1) (see FIG. 14) is maintained between adjacent staplepockets (242 a, 242 b, 242 c) for consistent overlap in the presentexample. As used herein, the term “overlap” is intended to include onefeature overlapping with another in at least one direction. Thus, afeature may be offset from another feature and still overlap asdescribed herein in the event that these features overlap in at leastone plane, such as a transverse plane including the transversedirection. While exemplary cartridge body (234) includes a variety ofstaple pockets (242 a, 242 b, 242 c) with staples (244 a, 244 b, 244 c)in order to accommodate the arcuate portion (230) as discussed below inadditional detail, it should be understood that the configuration ofstaple cartridge (218) may be varied in numerous ways. Other suitableforms that staple cartridge (218) may take will be apparent to those ofordinary skill in the art in view of the teachings herein.

As best seen in FIG. 12, anvil (224) of the present example has aplurality of staple forming pockets (246 a, 246 b, 246 c). Each stapleforming pocket (246 a, 246 b, 246 c) is positioned to lie over acorresponding staple pocket (242 a, 242 b, 242 c) of staple cartridge(218) when anvil (224) is in a closed position. Staple forming pockets(246 a, 246 b, 246 c) are configured to deform each leg (248) of staples(244 a, 244 b, 244 c) when staples (244 a, 244 b, 244 c) are driventhrough tissue and into anvil (224). In particular, staple formingpockets (246 a, 246 b, 246 c) are configured to bend legs (248) ofstaples (244 a, 244 b, 244 c) to secure the formed staples (244 a, 244b, 244 c) in the tissue. Other suitable forms that anvil (224) may takewill be apparent to those of ordinary skill in the art in view of theteachings herein.

As shown in FIG. 13, staple cartridge (218) includes staple row drivers(252) and a cross staple driver (254) positioned in staple pockets (242a, 242 b, 242 c), underneath corresponding sets of staples (244 a, 244b, 244 c), and above tray (not shown). As will be described in greaterdetail below, staple drivers (252, 254) are operable to translateupwardly in staple pockets (242 a, 242 b, 242 c) to thereby drivestaples (244 a, 244 b, 244 c) upwardly through staple pockets (242 a,242 b, 242 c) and into engagement with anvil (224). Staple drivers (252,254) are driven upwardly by a distally translating wedge sled (256),which is captured between cartridge body (234) and tray (not shown), andwhich translates longitudinally through cartridge body (234) along a camslot (257). Wedge sled (256) includes a cam ramp (258) having a leadingcam surface (260), an intermediate cam surface (262), and a trailing camsurface (264). By way of example only, leading cam surface (260) may beangled at approximately 45° relative to a horizontal plane; andintermediate cam surface (262) may be angled at approximately 22°relative to a horizontal plane. Alternatively, any other suitable anglesmay be used. Cam ramp (258) is generally configured to engage stapledrivers (252, 254) and thereby drive staple drivers (252, 254) upwardlyas wedge sled (256) translates longitudinally through staple cartridge(218) from a proximal sled position to a distal sled position. Forinstance, when wedge sled (256) is in the proximal sled position, stapledrivers (252, 254) are in downward positions and staples (244 a, 244 b,244 c) are located in staple pockets (442) below deck (238).

Wedge sled (256) is driven distally by a translating member (266). Byway of example only, translating member (266) may be translated distallyby actuating trigger (26)). Translating member (266) may thus operate ina manner similar to firing beam (82) described above, though translatingmember (266) lacks a cutting edge (84) and is unable to otherwise severtissue. As wedge sled (256) is driven to the distal sled position bytranslating member (266), wedge sled (256) drives staple drivers (252,254) upwardly, thereby driving staples (244 a, 244 b, 244 c) out ofstaple pockets (242 a, 242 b, 242 c) and into staple forming pockets(246 a, 246 b, 246 c). Thus, staple drivers (252, 254) translate alongcorresponding vertical planes as wedge sled (256) translates along ahorizontal plane.

1. Exemplary Arcuate Portion and Overlapping Predetermined StaplePattern of Staple Cartridge

As discussed above, end effector (212) includes arcuate portion (230),along which left and right rows of staple pockets (242 a, 242 b, 242 c)extend through deck (238). Exemplary staple cartridge (218) shown inFIG. 13 and FIG. 14 curves to the right, and, as such, the right row ofstaple pockets (242 a) is positioned radially inwardly from centerline(233), whereas the left row of staple pockets (242 b) is positionedradially outwardly from centerline (233). In addition, staple pockets(242 a) in linear portion (228) and in the right row have a crowndimension (C1) to accommodate staples (244 a). Thus, a consistent gap(G1) is maintained between adjacent staple pockets (242 a) in the row ofthe inner curve, for consistent overlap in the transverse direction withstaple pockets (242 b) in the row of the outer curve.

However, because these staple pockets (242 a, 242 b) follow thecurvature of arcuate portion (230) on each side of centerline (233), theleft or outer row of staple pockets (242 b) defines an elongated arcrelative to the shorter arc, which is defined by the right or inner rowof staple pockets (242 a). Each staple pocket (242 b) and staple (244 b)within arcuate portion (230) of the left or outer row is thus elongatedwith an elongated crown dimension (C2) in order to maintain consistentgap (G1) and overlap with the adjacent staple pockets (242 a) andstaples (244 a). Effectively, a crown (282 b) of each elongated staple(242 b) is longer than a crown (282 a) of each staple (242 a) to accountfor the elongated arc of the left or outer row of staple pockets (242b). Of course, it will be appreciated that other arrangements of staplepockets and associated staples may be used accordingly. For example, oneor more staples may be shortened relative to other staples (244 a) inlinear portion (228) to account for length differences between arcingrows of staple pockets.

Furthermore, while many of these above features have been describedspecifically with respect to lower jaw (216), it will be appreciatedthat corresponding linear portion (228) and arcuate portion (230) arealso included with upper jaw (212) (see FIG. 11). To this end, anvil(224) (see FIG. 11) also includes staple forming pockets (246 a, 246 b)(see FIG. 11) that respectively correspond to staple pockets (242 a, 242b) and include elongated crown dimension (C2) for forming staples (244b) with elongated crown (282 b). Thus, the geometry of upper jaw (212)complements the geometry of lower jaw (216).

2. Exemplary Method of Tissue Resection

FIGS. 15A-15F show one example of using end effector (212) to resecttissue, such as a liver parenchyma tissue (310), and to ligate a vesselor duct (316) therein. As noted above, vessel or duct (316) may comprisea hepatic vein or a hepatic artery. It should also be understood thatthe method may further include the use of end effector (212) to ligateother vessels such as the portal vein and extrahepatic vessels, etc.

As shown in FIG. 15B, the operator positions end effector (212) suchthat tissue (310), including vessel or duct (316), is located betweenlower and upper jaws (220, 222). The operator then compresses tissue(310) between upper and lower crush surfaces (214, 216) of upper andlower jaws (220, 222), respectively, to deliver the predetermined crushpressure to tissue (310). By way of example only, jaws (220, 222) may beactuated in this manner by pivoting trigger (24) toward pistol grip(22). It should be understood that jaws (220, 222) need not necessarilybe actuated to a fully closed configuration. In some instances, theoperator may rely on tactile feedback through trigger (24) and pistolgrip (22) to determine whether the operator has achieved a desired gapbetween jaws (220, 222) to suitably crush tissue (310) withoutundesirably damaging vessel or duct (316). In addition or in thealternative, the operator may rely on visual feedback.

In any case, the crush pressure applied by jaws (220, 222) effectivelysevers tissue (310), and the operator then removes end effector (212)from tissue (310) to view whether or not any vessels or ducts (316) arepresent. As shown in FIG. 15C, vessel or duct (316) remains intact andis left exposed, extending between severed portions of tissue (310).

In some instances, the operator may leave vessel or duct (316) intact.However, in the present example, the operator ligates vessel or duct(316) to complete the resection of a severed portion of tissue (310), asshown in FIG. 15D and FIG. 15E. Ligation includes placement of at leastsome of overlapping staples (244 a, 244 b, 244 c) within vessel or duct(316) as discussed above in greater detail. It should therefore beunderstood that the same end effector (212) may be used to crush (andthereby sever) tissue (310) of the liver and also ligate a vessel orduct (316) in the tissue (310). In the present example, after ligationof vessel or duct (316), the operator removes end effector (212) fromliver tissue (310) and severs vessel or duct (316) with another surgicalinstrument (not shown) known in the art for cutting tissue, such as aconventional blade or shears, etc. Thereby, the operator completesresection of a right portion of tissue (310) and the correspondingportion of the vessel or duct (316), as shown in FIG. 15F. The appliedstaples (244 a) seal the severed end (318) of the vessel or duct (316).

As described above, the operator removes end effector (212) for viewingvessel (316) as shown in FIG. 15C. Alternatively, the operator may applythe predetermined crush pressure (or as determined based on tactileand/or visual feedback as noted above), as shown in FIG. 15B, andimmediately thereafter ligate any tissue remaining therein, such asvessel or duct (316). As such, it is not necessary to view such tissue,but the operator may find such viewing desirable in one or more liverresection procedures. It will be appreciated that the above describedresection is merely illustrative and not limited to liver tissue.Alternatively, tissue resection with end effector (212) may be performedon other tissues within the patient as desired by the user.

III. Exemplary Combinations

The following examples relate to various non-exhaustive ways in whichthe teachings herein may be combined or applied. It should be understoodthat the following examples are not intended to restrict the coverage ofany claims that may be presented at any time in this application or insubsequent filings of this application. No disclaimer is intended. Thefollowing examples are being provided for nothing more than merelyillustrative purposes. It is contemplated that the various teachingsherein may be arranged and applied in numerous other ways. It is alsocontemplated that some variations may omit certain features referred toin the below examples. Therefore, none of the aspects or featuresreferred to below should be deemed critical unless otherwise explicitlyindicated as such at a later date by the inventors or by a successor ininterest to the inventors. If any claims are presented in thisapplication or in subsequent filings related to this application thatinclude additional features beyond those referred to below, thoseadditional features shall not be presumed to have been added for anyreason relating to patentability.

Example 1

A surgical instrument for treating a tissue of a patient, comprising:(a) a shaft assembly; (b) an end effector extending from the shaftassembly along a jaw centerline, the end effector comprising: (i) afirst jaw having an anvil configured to form a plurality of staplespressed against the anvil, and (ii) a second jaw, wherein the first andsecond jaws are configured to transition between an open configurationand a closed configuration; and (c) a staple cartridge received withinthe second jaw, wherein the staple cartridge and the end effector havean arcuate portion, the staple cartridge comprising: (i) a deck facingthe anvil, wherein the deck defines a plurality of staple openings,wherein the plurality of staple openings comprises an outer row ofstaple openings positioned radially outward from the centerline in thearcuate portion and an inner row of staple openings positioned radiallyinward from the centerline in the arcuate portion, and (ii) a pluralityof staples positioned respectively within the plurality of stapleopenings, wherein the plurality of staples include an outer set ofstaples and an inner set of staples for respective receipt within theouter and inner rows of staple openings, wherein at least one staple ofthe outer set of staples has an elongated crown relative to the innerset of staples such that the outer set of staples are configured tooverlap with the inner set of staples in a direction transverse to thecenterline.

Example 2

The surgical instrument of Example 1, wherein the end effector, thestaple cartridge, and the centerline have a straight portion, whereinthe straight portion extends to the arcuate portion.

Example 3

The surgical instrument of Example 2, wherein the plurality of stapleopenings comprises a first row of staple openings and a second row ofstaple openings, wherein the first and second rows of staple openingsare positioned on respective sides of centerline and are formed on thedeck in the straight portion.

Example 4

The surgical instrument of any one or more of Examples 1 through 3,wherein the outer row of staple openings defines a plurality of outergaps between the plurality of staple openings, wherein the inner row ofstaple openings defines a plurality of inner gaps between the pluralityof staple openings, wherein the inner gaps and outer gaps have anequivalent elongation.

Example 5

The surgical instrument of any one or more of Examples 1 through 4,wherein the plurality of staple openings further include at least onestaple opening extending between the outer and inner rows of stapleopenings, wherein the at least one staple opening extending between theouter and inner rows of staple opening straddles the centerline.

Example 6

The surgical instrument of Example 5, wherein the at least one stapleopening that straddles the centerline is a distal-most staple opening inthe deck.

Example 7

The surgical instrument of any one or more of Examples 1 through 6,wherein the first jaw comprises a first crush surface extendinggenerally parallel with the centerline, wherein the first crush surfaceis configured to receive tissue thereagainst, wherein the second jawcomprises a second crush surface extending generally parallel with thecenterline, wherein the second crush surface is configured to receivethe tissue thereagainst, wherein the first and second crush surfaces areconfigured to compress tissue therebetween with a crush pressureconfigured to sever the tissue along the first and second crushsurfaces.

Example 8

The surgical instrument of Example 7, wherein the end effector, thestaple cartridge, and the centerline have a straight portion, whereinthe straight portion extends to the arcuate portion, and wherein thefirst and second crush surfaces extend along the straight and arcuateportions.

Example 9

The surgical instrument of Example 8, wherein the second crush surfaceis formed on the deck of the staple cartridge.

Example 10

The surgical instrument of any one or more of Examples 1 through 9,wherein the arcuate portion extends to a distal tip of the end effector,and wherein at least a portion of the end effector tapers inwardlytoward the distal tip.

Example 11

The surgical instrument of any one or more of Examples 1 through 10,wherein staple cartridge further comprises a wedge sled configured toslide proximate to the deck from a proximal sled position to a distalsled position, and wherein the wherein the distal sled position is inthe arcuate portion of the end effector.

Example 12

The surgical instrument of Example 11, wherein the staple cartridgefurther comprises a slot positioned below the deck, wherein the slotextends along the centerline at least partially through the arcuateportion.

Example 13

The surgical instrument of Example 12, wherein the staple cartridgefurther comprises a driver assembly having a first driver and a seconddriver, the first driver receiving a first staple of the plurality ofstaples, and the second driver receiving a second staple of theplurality of staples, wherein the driver assembly is configured to beengaged by the wedge sled sliding toward the distal sled position andforced toward the first jaw, thereby forcing the first and secondstaples toward the anvil for formation in tissue.

Example 14

The surgical instrument of Example 13, wherein the wedge sled comprisesa cam ramp, the cam ramp being positioned on the centerline within theslot and configured to engage the driver assembly and force the driverassembly toward the first jaw.

Example 15

The surgical instrument of Example 14, further comprising a translatingmember engaged with wedge sled and configured to be actuated to drivethe wedge sled from the proximal sled position toward the distal sledposition, wherein translating member and wedge sled are configured tofollow the centerline along the slot through the arcuate portion.

IV. Miscellaneous

It should be understood that any one or more of the teachings,expressions, embodiments, examples, etc. described herein may becombined with any one or more of the other teachings, expressions,embodiments, examples, etc. that are described herein. Theabove-described teachings, expressions, embodiments, examples, etc.should therefore not be viewed in isolation relative to each other.Various suitable ways in which the teachings herein may be combined willbe readily apparent to those of ordinary skill in the art in view of theteachings herein. Such modifications and variations are intended to beincluded within the scope of the claims.

It should be appreciated that any patent, publication, or otherdisclosure material, in whole or in part, that is said to beincorporated by reference herein is incorporated herein only to theextent that the incorporated material does not conflict with existingdefinitions, statements, or other disclosure material set forth in thisdisclosure. As such, and to the extent necessary, the disclosure asexplicitly set forth herein supersedes any conflicting materialincorporated herein by reference. Any material, or portion thereof, thatis said to be incorporated by reference herein, but which conflicts withexisting definitions, statements, or other disclosure material set forthherein will only be incorporated to the extent that no conflict arisesbetween that incorporated material and the existing disclosure material.

Versions of the devices described above may have application inconventional medical treatments and procedures conducted by a medicalprofessional, as well as application in robotic-assisted medicaltreatments and procedures. By way of example only, various teachingsherein may be readily incorporated into a robotic surgical system suchas the DAVINCI™ system by Intuitive Surgical, Inc., of Sunnyvale, Calif.Similarly, those of ordinary skill in the art will recognize thatvarious teachings herein may be readily combined with various teachingsof any of the following: U.S. Pat. No. 5,792,135, entitled “ArticulatedSurgical Instrument For Performing Minimally Invasive Surgery WithEnhanced Dexterity and Sensitivity,” issued Aug. 11, 1998, thedisclosure of which is incorporated by reference herein; U.S. Pat. No.5,817,084, entitled “Remote Center Positioning Device with FlexibleDrive,” issued Oct. 6, 1998, the disclosure of which is incorporated byreference herein; U.S. Pat. No. 5,878,193, entitled “Automated EndoscopeSystem for Optimal Positioning,” issued Mar. 2, 1999, the disclosure ofwhich is incorporated by reference herein; U.S. Pat. No. 6,231,565,entitled “Robotic Arm DLUS for Performing Surgical Tasks,” issued May15, 2001, the disclosure of which is incorporated by reference herein;U.S. Pat. No. 6,783,524, entitled “Robotic Surgical Tool with UltrasoundCauterizing and Cutting Instrument,” issued Aug. 31, 2004, thedisclosure of which is incorporated by reference herein; U.S. Pat. No.6,364,888, entitled “Alignment of Master and Slave in a MinimallyInvasive Surgical Apparatus,” issued Apr. 2, 2002, the disclosure ofwhich is incorporated by reference herein; U.S. Pat. No. 7,524,320,entitled “Mechanical Actuator Interface System for Robotic SurgicalTools,” issued Apr. 28, 2009, the disclosure of which is incorporated byreference herein; U.S. Pat. No. 7,691,098, entitled “Platform Link WristMechanism,” issued Apr. 6, 2010, the disclosure of which is incorporatedby reference herein; U.S. Pat. No. 7,806,891, entitled “Repositioningand Reorientation of Master/Slave Relationship in Minimally InvasiveTelesurgery,” issued Oct. 5, 2010, the disclosure of which isincorporated by reference herein; U.S. Pub. No. 2013/0012957, entitled“Automated End Effector Component Reloading System for Use with aRobotic System, published Jan. 10, 2013, the disclosure of which isincorporated by reference herein; U.S. Pub. No. 2012/0199630, entitled“Robotically-Controlled Surgical Instrument with Force-FeedbackCapabilities,” published Aug. 9, 2012, the disclosure of which isincorporated by reference herein; U.S. Pub. No. 2012/0132450, entitled“Shiftable Drive Interface for Robotically-Controlled Surgical Tool,”published May 31, 2012, the disclosure of which is incorporated byreference herein; U.S. Pub. No. 2012/0199633, entitled “SurgicalStapling Instruments with Cam-Driven Staple Deployment Arrangements,”published Aug. 9, 2012, the disclosure of which is incorporated byreference herein; U.S. Pub. No. 2012/0199631, entitled“Robotically-Controlled Motorized Surgical End Effector System withRotary Actuated Closure Systems Having Variable Actuation Speeds,”published Aug. 9, 2012, the disclosure of which is incorporated byreference herein; U.S. Pub. No. 2012/0199632, entitled“Robotically-Controlled Surgical Instrument with SelectivelyArticulatable End Effector,” published Aug. 9, 2012, the disclosure ofwhich is incorporated by reference herein; U.S. Pub. No. 2012/0203247,entitled “Robotically-Controlled Surgical End Effector System,”published Aug. 9, 2012, the disclosure of which is incorporated byreference herein; U.S. Pub. No. 2012/0211546, entitled “Drive Interfacefor Operably Coupling a Manipulatable Surgical Tool to a Robot,”published Aug. 23, 2012; U.S. Pub. No. 2012/0138660, entitled“Robotically-Controlled Cable-Based Surgical End Effectors,” publishedJun. 7, 2012, the disclosure of which is incorporated by referenceherein; and/or U.S. Pub. No. 2012/0205421, entitled“Robotically-Controlled Surgical End Effector System with RotaryActuated Closure Systems,” published Aug. 16, 2012, the disclosure ofwhich is incorporated by reference herein.

Versions of the devices described above may be designed to be disposedof after a single use, or they can be designed to be used multipletimes. Versions may, in either or both cases, be reconditioned for reuseafter at least one use. Reconditioning may include any combination ofthe steps of disassembly of the device, followed by cleaning orreplacement of particular pieces, and subsequent reassembly. Inparticular, some versions of the device may be disassembled, and anynumber of the particular pieces or parts of the device may beselectively replaced or removed in any combination. Upon cleaning and/orreplacement of particular parts, some versions of the device may bereassembled for subsequent use either at a reconditioning facility, orby a operator immediately prior to a procedure. Those skilled in the artwill appreciate that reconditioning of a device may utilize a variety oftechniques for disassembly, cleaning/replacement, and reassembly. Use ofsuch techniques, and the resulting reconditioned device, are all withinthe scope of the present application.

By way of example only, versions described herein may be sterilizedbefore and/or after a procedure. In one sterilization technique, thedevice is placed in a closed and sealed container, such as a plastic orTYVEK bag. The container and device may then be placed in a field ofradiation that can penetrate the container, such as gamma radiation,x-rays, or high-energy electrons. The radiation may kill bacteria on thedevice and in the container. The sterilized device may then be stored inthe sterile container for later use. A device may also be sterilizedusing any other technique known in the art, including but not limited tobeta or gamma radiation, ethylene oxide, or steam.

Having shown and described various embodiments of the present invention,further adaptations of the methods and systems described herein may beaccomplished by appropriate modifications by one of ordinary skill inthe art without departing from the scope of the present invention.Several of such potential modifications have been mentioned, and otherswill be apparent to those skilled in the art. For instance, theexamples, embodiments, geometries, materials, dimensions, ratios, steps,and the like discussed above are illustrative and are not required.Accordingly, the scope of the present invention should be considered interms of the following claims and is understood not to be limited to thedetails of structure and operation shown and described in thespecification and drawings.

I/We claim:
 1. A surgical instrument for treating a tissue of a patient,comprising: (a) a shaft assembly; (b) an end effector extending from theshaft assembly along a jaw centerline, the end effector comprising: (i)a first jaw having an anvil configured to form a plurality of staplespressed against the anvil, and (ii) a second jaw, wherein the first andsecond jaws are configured to transition between an open configurationand a closed configuration; and (c) a staple cartridge received withinthe second jaw, wherein the staple cartridge and the end effector havean arcuate portion, the staple cartridge comprising: (i) a deck facingthe anvil, wherein the deck defines a plurality of staple openings,wherein the plurality of staple openings comprises an outer row ofstaple openings positioned radially outward from the centerline in thearcuate portion and an inner row of staple openings positioned radiallyinward from the centerline in the arcuate portion, and (ii) a pluralityof staples positioned respectively within the plurality of stapleopenings, wherein the plurality of staples include an outer set ofstaples and an inner set of staples for respective receipt within theouter and inner rows of staple openings, wherein at least one staple ofthe outer set of staples has an elongated crown relative to the innerset of staples such that the outer set of staples are configured tooverlap with the inner set of staples in a direction transverse to thecenterline.
 2. The surgical instrument of claim 1, wherein the endeffector, the staple cartridge, and the centerline have a straightportion, wherein the straight portion extends to the arcuate portion. 3.The surgical instrument of claim 2, wherein the plurality of stapleopenings comprises a first row of staple openings and a second row ofstaple openings, wherein the first and second rows of staple openingsare positioned on respective sides of centerline and are formed on thedeck in the straight portion.
 4. The surgical instrument of claim 1,wherein the outer row of staple openings defines a plurality of outergaps between the plurality of staple openings, wherein the inner row ofstaple openings defines a plurality of inner gaps between the pluralityof staple openings, wherein the inner gaps and outer gaps have anequivalent elongation.
 5. The surgical instrument of claim 1, whereinthe plurality of staple openings further include at least one stapleopening extending between the outer and inner rows of staple openings,wherein the at least one staple opening extending between the outer andinner rows of staple opening straddles the centerline.
 6. The surgicalinstrument of claim 5, wherein the at least one staple opening thatstraddles the centerline is a distal-most staple opening in the deck. 7.The surgical instrument of claim 1, wherein the first jaw comprises afirst crush surface extending generally parallel with the centerline,wherein the first crush surface is configured to receive tissuethereagainst, wherein the second jaw comprises a second crush surfaceextending generally parallel with the centerline, wherein the secondcrush surface is configured to receive the tissue thereagainst, whereinthe first and second crush surfaces are configured to compress tissuetherebetween with a crush pressure configured to sever the tissue alongthe first and second crush surfaces.
 8. The surgical instrument of claim7, wherein the end effector, the staple cartridge, and the centerlinehave a straight portion, wherein the straight portion extends to thearcuate portion, and wherein the first and second crush surfaces extendalong the straight and arcuate portions.
 9. The surgical instrument ofclaim 8, wherein the second crush surface is formed on the deck of thestaple cartridge.
 10. The surgical instrument of claim 1, wherein thearcuate portion extends to a distal tip of the end effector, and whereinat least a portion of the end effector tapers inwardly toward the distaltip.
 11. The surgical instrument of claim 1, wherein staple cartridgefurther comprises a wedge sled configured to slide proximate to the deckfrom a proximal sled position to a distal sled position, and wherein thewherein the distal sled position is in the arcuate portion of the endeffector.
 12. The surgical instrument of claim 11, wherein the staplecartridge further comprises a slot positioned below the deck, whereinthe slot extends along the centerline at least partially through thearcuate portion.
 13. The surgical instrument of claim 12, wherein thestaple cartridge further comprises a driver assembly having a firstdriver and a second driver, the first driver receiving a first staple ofthe plurality of staples, and the second driver receiving a secondstaple of the plurality of staples, wherein the driver assembly isconfigured to be engaged by the wedge sled sliding toward the distalsled position and forced toward the first jaw, thereby forcing the firstand second staples toward the anvil for formation in tissue.
 14. Thesurgical instrument of claim 13, wherein the wedge sled comprises a camramp, the cam ramp being positioned on the centerline within the slotand configured to engage the driver assembly and force the driverassembly toward the first jaw.
 15. The surgical instrument of claim 14,further comprising a translating member engaged with wedge sled andconfigured to be actuated to drive the wedge sled from the proximal sledposition toward the distal sled position, wherein translating member andwedge sled are configured to follow the centerline along the slotthrough the arcuate portion.